@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_head {
  this: np:hasAssertion dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_assertion;
    np:hasProvenance dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_provenance;
    np:hasPublicationInfo dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_assertion a np:Assertion .
  
  dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_provenance a np:Provenance .
  
  dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0032463 a ncit:C7057 .
  
  dgn-gda:DGN949cbb7dfed25bfe38f8d9943230f081 sio:SIO_000628 miriam-gene:3717, lld:C0032463;
    a sio:SIO_001121 .
}

dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_provenance {
  dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_assertion dcterms:description
      "[For instance, the presence of a JAK2 mutation is now considered conditio sine qua non for the diagnosis of PV and the World Health Organization classification system has recently revised its diagnostic criteria for PV, ET, and PMF to include JAK2 and MPL mutations as clonal markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:18429051;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP667231.RAlyCFABA6ZVB2GgBnWz7KAm7tVl9GrJAYmtH5X8tzKEY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:47+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}